chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117574602117574603GA13GENIChomozygous116672000
8117575608117575609GA17GENIChomozygous116672002
8117576152117576153CT31GENIChomozygous116672004
8117579060117579061TC8GENIChomozygous116988179
8117579086117579087TC7GENIChomozygous116672006
8117580189117580190AC25GENIChomozygous116672008
8117580267117580268GA19GENIChomozygous116672010
8117581875117581876TC19GENIChomozygous116672012
8117582166117582167CT18GENIChomozygous116672014
8117590581117590582TG17GENIChomozygous116672018
8117593788117593789CT10GENICpossibly homozygous117982363
8117596942117596943AC24GENIChomozygous116672022
8117597287117597288CA7GENIChomozygous116672024
8117597825117597826AG25GENIChomozygous116672026
8117599006117599007AG22GENIChomozygous116672028
8117599030117599031AG18GENIChomozygous116672030